MAUDE Adverse Event Report: ATRIUM MEDICAL CORPORATION ICAST COVERED STENT SYSTEM, 10MMX38MMX120CM; ILIAC COVERED STENT, ARTERIAL

Model Number	42038
Medical Device Problem Code	Failure to Advance (2524)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/06/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that during reintervention with a cook zbis for treatment of a type 1b endoleak from a prior terumo graft, an icast stent was delivered through high flex ansel sheath positioned in the left hypogastric branch of the cook zbis.The icast stent did not make the bifurcation turn and was therefore removed.Two vbx stents were placed without difficulty.There was no harm or adverse event reported.
Additional Manufacturer Narrative
Due to character restrictions in following field: d10: concomitant products: cook zbis, terumo graft, high flex ansel sheath e1: event site address line: (b)(6).A supplemental report will be submitted upon completion of our investigation.
Event or Problem Description
N/a.
Additional Manufacturer Narrative
Additional information: a2, e1 (event site email, event site telephone, initial reporter).

• Brand Name: ICAST COVERED STENT SYSTEM, 10MMX38MMX120CM
• Common Device Name: ILIAC COVERED STENT, ARTERIAL
• Manufacturer (Section D): ATRIUM MEDICAL CORPORATION; 40 continental blvd; merrimack NH
• Manufacturer (Section G): ATRIUM MEDICAL CORPORATION; 40 continental blvd; merrimack NH
• Manufacturer Contact: lori gosselin ; 40 continental blvd; merrimack, NH
• MDR Report Key: 24789463
• Report Number: 3011175548-2026-000003
• Device Sequence Number: 18621657
• Product Code: PRL
• UDI-Device Identifier: 00650862420388
• UDI-Public: (01)00650862420388(17)281111
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: P120003
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/22/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 42038
• Device Catalogue Number: 42038
• Device Lot Number: 525631
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/11/2026
• Supplement Date Received by Manufacturer: 04/11/2026; 05/20/2026
• Initial Report FDA Received Date: 04/06/2026
• Supplement Report FDA Received Date: 04/14/2026; 05/22/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/12/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: COOK ZBIS, TERUMO GRAFT
• Patient Age: 68 YR
• Patient Sex: Female